EP1153900A2 - Process for producing magnetoplumbite-type ferrite sintered magnet - Google Patents

Process for producing magnetoplumbite-type ferrite sintered magnet Download PDF

Info

Publication number
EP1153900A2
EP1153900A2 EP01304165A EP01304165A EP1153900A2 EP 1153900 A2 EP1153900 A2 EP 1153900A2 EP 01304165 A EP01304165 A EP 01304165A EP 01304165 A EP01304165 A EP 01304165A EP 1153900 A2 EP1153900 A2 EP 1153900A2
Authority
EP
European Patent Office
Prior art keywords
ferrite particles
magnetoplumbite structure
sintered magnet
magnetoplumbite
particles
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
EP01304165A
Other languages
German (de)
French (fr)
Other versions
EP1153900A3 (en
Inventor
Mitsuharu Tabuchi
Tomonari Takeuchi
Hiroyuki Kageyama
Tatsuya Nakamura
Yoji Okano
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
National Institute of Advanced Industrial Science and Technology AIST
Toda Kogyo Corp
Original Assignee
National Institute of Advanced Industrial Science and Technology AIST
Toda Kogyo Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by National Institute of Advanced Industrial Science and Technology AIST, Toda Kogyo Corp filed Critical National Institute of Advanced Industrial Science and Technology AIST
Publication of EP1153900A2 publication Critical patent/EP1153900A2/en
Publication of EP1153900A3 publication Critical patent/EP1153900A3/en
Withdrawn legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B35/00Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
    • C04B35/622Forming processes; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
    • C04B35/64Burning or sintering processes
    • C04B35/645Pressure sintering
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B35/00Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
    • C04B35/01Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics
    • C04B35/26Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics based on ferrites
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01FMAGNETS; INDUCTANCES; TRANSFORMERS; SELECTION OF MATERIALS FOR THEIR MAGNETIC PROPERTIES
    • H01F41/00Apparatus or processes specially adapted for manufacturing or assembling magnets, inductances or transformers; Apparatus or processes specially adapted for manufacturing materials characterised by their magnetic properties
    • H01F41/02Apparatus or processes specially adapted for manufacturing or assembling magnets, inductances or transformers; Apparatus or processes specially adapted for manufacturing materials characterised by their magnetic properties for manufacturing cores, coils, or magnets
    • H01F41/0253Apparatus or processes specially adapted for manufacturing or assembling magnets, inductances or transformers; Apparatus or processes specially adapted for manufacturing materials characterised by their magnetic properties for manufacturing cores, coils, or magnets for manufacturing permanent magnets
    • H01F41/0266Moulding; Pressing

Definitions

  • the present invention relates to a process for producing a magnetoplumbite-type ferrite sintered magnet, and more particularly, to a process for producing a magnetoplumbite-type ferrite sintered magnet (sintered magnet composed of ferrite particles with magnetoplumbite structure) having a large density and a small crystallite size, at a low temperature for a short period of time.
  • the sintered magnet composed of ferrite particles with magnetoplumbite structures have advantages such as good chemical stability and low production costs and, therefore, have been widely used in various applications such as motors, electronic devices and the like.
  • the magnetoplumbite-type ferrite sintered magnet has been produced by the following method. First, raw materials such as oxides and carbonates containing metal elements as constituents of ferrite particles with magnetoplumbite structure, are mixed together. The resultant mixture is calcined in an electric furnace and then pulverized. The obtained particles are wet-molded under a magnetic field. Then, the obtained molded product is sintered in air at a temperature of 1180 to 1,230°C to produce the magnetoplumbite-type ferrite sintered magnet (Japanese Patent Application Laid-Open (KOKAI) No. 10-149910(1998)).
  • the present inventors' earnest studies to solve the above problem it has been found that by sintering ferrite particles with magnetoplumbite structure under pressure while applying an electric current thereto, the obtained sintered magnet composed of ferrite particles with magnetoplumbite structure can exhibit a large magnetic flux density and a high coercive force.
  • the present invention has been attained based on the above finding.
  • An object of the present invention is to provide a process for producing a sintered magnet composed of ferrite particles with magnetoplumbite structure exhibiting a larger magnetic flux density and a high coercive force, at a relatively low temperature for a short period of time.
  • a process for producing a sintered magnet composed of ferrite particles with magnetoplumbite structure comprising:
  • a process for producing a sintered magnet composed of ferrite particles with magnetoplumbite structure comprising:
  • a process for producing a sintered magnet composed of ferrite particles with magnetoplumbite structure comprising:
  • the ferrite particles with magnetoplumbite structure used in the present invention have a composition represented by the formula: SrO•nFe 2 O 3 wherein a part of Sr may be substituted with Ba, Pb, La, Nd or Pr; a part of Fe may be substituted with Ni, Mn, Ti, Co, Zn, Al or Sn; and n is 5.5 to 6.2.
  • the upper limit of Sr amount substituted with Ba, Pb, La, Nd or Pr is preferably 70 mol%, more preferably 50 mol %, and the upper limit of Fe amount substituted with Ni, Mn, Ti, Co, Zn, Al or Sn is preferably 40 mol%, more preferably 30 mol%.
  • composition of the ferrite particles with magnetoplumbite structure does not satisfy the above-specified formula, it is difficult to obtain the aimed sintered magnet composed of ferrite particles with magnetoplumbite structure having a large magnetic flux density and a high coercive force.
  • the ferrite particles with magnetoplumbite structure may be produced by a known wet-method, more specifically, by mixing a strontium compound and an iron compound together in a solution so as to constitute the above-specified composition; adding sodium hydroxide, potassium hydroxide, etc. to the mixture, thereby causing Sr 2+ ions and Fe 3+ ions to be precipitated; and then heating the resultant precipitates in an autoclave at about 200°C for subjecting the particles to hydrothermal treatment.
  • fine ferrite particles with magnetoplumbite structure obtained by mixing a strontium compound and an iron compound together in a solution so as to constitute the above-specified composition; adding sodium carbonate, potassium carbonate, etc. to the mixture, thereby causing Sr 2+ ions and Fe 3+ ions to be precipitated; and then calcining the resultant precipitates at a temperature of about 700 to 1,000°C.
  • the ferrite particles with magnetoplumbite structure produced by the wet-method according to the present invention have an average particle diameter of usually not more than 0.9 ⁇ m, preferably 0.1 to 0.9 ⁇ m.
  • the average particle diameter is more than 0.9 ⁇ m, the obtained sintered magnet has a crystallite size larger than its critical single domain particle diameter, so that the coercive force thereof tends to be deteriorated.
  • the average thickness of the ferrite particles with magnetoplumbite structure produced by the wet-method according to the present invention is preferably 0.005 to 0.6 ⁇ m, more preferably 0.01 to 0.45 ⁇ m.
  • a growth inhibitor such as SiO 2 and/or CaCO 3 may be mixed with the ferrite particles with magnetoplumbite structure using a ball mill, etc. before sintering.
  • the amount of SiO 2 added is preferably not more than 2 % by weight, more preferably not more than 1 % by weight based on the weight of the ferrite particles with magnetoplumbite structure.
  • the amount of CaCO 3 added is preferably not more than 2.5 % by weight, more preferably not more than 1.5 % by weight based on the weight of the ferrite particles with magnetoplumbite structure.
  • the amount of mixture of SiO 2 and CaCO 3 added is preferably not more than 4.5 % by weight, more preferably not more than 2.5 % by weight based on the weight of the ferrite particles with magnetoplumbite structure.
  • the ferrite particles with magnetoplumbite structure produced by the wet-method are then filled in a mold, and supplied with an electric current under pressure, thereby sintering the ferrite particles with magnetoplumbite structure.
  • this method is called "spark plasma sintering method".
  • materials of the mold used in the above sintering method graphite or the like may be used because of a high electrical conductivity, a low chemical reactivity with ferrite and inexpensiveness thereof.
  • the pressure applied to the ferrite particles with magnetoplumbite structure filled in the mold is usually 5 to 500 MPa, preferably 10 to 200 MPa when measured at the surface of a sample compact in the mold.
  • the applied pressure is less than 5 MPa, it is difficult to sinter the ferrite particles with magnetoplumbite structure.
  • the obtained sintered magnet has a density of less than 5,000 kg/m 3 , resulting in insufficient strength thereof.
  • the sintered magnet composed of ferrite particles with magnetoplumbite structure having such a low density fails to show a large magnetic flux density.
  • the pressure of 500 MPa is sufficient to sinter the ferrite particles with magnetoplumbite structure. Therefore, in the consideration of economy, it is unnecessary to use such a large pressure exceeding 500 MPa.
  • the electric current applied to the ferrite particles with magnetoplumbite structure is usually 100 to 2,000 A, preferably 500 to 1,500 A.
  • the electric current applied is less than 100 A, it is difficult to sinter the ferrite particles with magnetoplumbite structure.
  • the obtained sintered magnet has a density of less than 5,000 kg/m 3 , resulting in insufficient strength thereof.
  • the sintered magnet composed of ferrite particles with magnetoplumbite structure having such a low density fails to show a large magnetic flux density.
  • the sintering of the ferrite particles with magnetoplumbite structure can sufficiently proceed by applying the electric current of 2,000 A thereto. Therefore, in the consideration of economy, it is unnecessary to apply such a large electric current exceeding 2,000 A.
  • the voltage applied to the ferrite particles with magnetoplumbite structure is usually 1 to 10 V, preferably 1 to 5 V.
  • the voltage applied is less than 1 V, it is difficult to sinter the ferrite particles with magnetoplumbite structure.
  • the obtained sintered magnet has a density of less than 5,000 kg/m 3 , resulting in insufficient strength thereof.
  • the sintered magnet composed of ferrite particles with magnetoplumbite structure having such a low density fails to show a large magnetic flux density.
  • the sintering of the ferrite particles with magnetoplumbite structure can sufficiently proceed by applying the voltage of 10 V thereto. Therefore, in the consideration of economy, it is unnecessary to apply such a large voltage exceeding 10 V.
  • the sintering temperature is usually 850 to 1,050°C, preferably 875 to 1,025°C.
  • the sintering temperature is less than 850°C, it is difficult to sinter the ferrite particles with magnetoplumbite structure.
  • the obtained sintered magnet has a density of less than 5,000 kg/m 3 , resulting in insufficient strength thereof.
  • the sintered magnet composed of ferrite particles with magnetoplumbite structure having such a low density fails to show a large magnetic flux density.
  • the sintering temperature is more than 1,050°C, the growth of the ferrite particles with magnetoplumbite structure proceeds excessively, so that the crystallite size thereof exceeds the critical single domain particle diameter (about 0.9 ⁇ m), resulting in deteriorated coercive force of the obtained sintered magnet.
  • the sintering time is usually 1 to 15 minutes, preferably 1 to 10 minutes.
  • the sintering time is less than one minute, it is difficult to sinter the ferrite particles with magnetoplumbite structure.
  • the obtained sintered magnet has a density of less than 5,000 kg/m 3 , resulting in insufficient strength thereof.
  • the sintered magnet composed of ferrite particles with magnetoplumbite structure having such a low density fails to show a large magnetic flux density.
  • the sintering time of 15 minutes is sufficient to sinter the ferrite particles with magnetoplumbite structure. Therefore, in the consideration of economy, it is unnecessary to use such a long sintering time beyond 15 minutes.
  • the sintering treatment may be usually conducted in a non-reducing atmosphere, preferably in an oxidative atmosphere.
  • the pressure of the specific atmosphere during the sintering treatment is not particularly restricted, and it is preferred that the sintering treatment be conducted under atmospheric pressure.
  • the ferrite particles with magnetoplumbite structure are sintered by the above spark plasma sintering method, it is possible to obtain the aimed sintered magnet composed of ferrite particles with magnetoplumbite structure capable of exhibiting a large density and a small crystallite size as well as a large magnetic flux density and a high coercive force.
  • the spark plasma is generated within the mold and directly acts between the particles, unlike the conventional method in which a molded product composed of the ferrite particles with magnetoplumbite structure is sintered in an electric furnace such as Fisher furnace at a temperature of more than 1,080°C for not less than 30 minutes.
  • an electric furnace such as Fisher furnace at a temperature of more than 1,080°C for not less than 30 minutes.
  • a sintered magnet composed of ferrite particles with magnetoplumbite structure having a crystallite size not more than the critical single domain particle diameter (0.9 ⁇ m), a density of not less than 5,000 kg/m 3 , preferably 5,000 to 5,150 kg/m 3 , a magnetization value of 60 to 70 Am 2 /kg, a coercive force of 100 to 400 kA/m and a magnetic flux density of 350 to 450 mT.
  • the ferrite particles with magnetoplumbite structure are sintered together at a relatively low temperature for a short period of time by the spark plasma sintering method, the growth of the ferrite particles with magnetoplumbite structure can be effectively inhibited. As a result, it is possible to obtain the aimed sintered magnet composed of ferrite particles with magnetoplumbite structure having a small crystallite size and a high density as well as a large magnetic flux density and a high coercive force.
  • An aqueous mixed solution containing SrCl 2 •6H 2 O and Fe(NO 3 ) 3 •9H 2 O was prepared such that the molar ratio of Fe 3+ to Sr 2+ was 11.4:1.
  • An aqueous NaOH solution was then added to the aqueous mixed solution in an amount not less than that required for neutralizing the Sr and Fe compounds so as to allow Sr 2+ ions and Fe 3+ ions to be precipitated.
  • the obtained precipitates were treated in an autoclave at 200°C under 20 atm for 5 hours.
  • the resultant reaction product was washed with water, filtered out and then dried, thereby obtaining ferrite particles with magnetoplumbite structure. It was confirmed that the thus obtained ferrite particles with magnetoplumbite structure had an average particle diameter of 0.25 ⁇ m and an average thickness of 0.08 ⁇ m.
  • An aqueous mixed solution containing SrCl 2 •6H 2 O and Fe(NO 3 ) 3 •9H 2 O was prepared such that the molar ratio of Fe 3+ to Sr 2+ was 11.4:1.
  • Na 2 CO 3 was added to the aqueous mixed solution in an amount not less than that required for neutralizing the Sr and Fe compounds so as to allow Sr 2+ ions and Fe 3+ ions to be precipitated.
  • the obtained precipitates were calcined in air at 1,000°C for 3 hours, thereby obtaining ferrite particles with magnetoplumbite structure. It was confirmed that the thus obtained ferrite particles with magnetoplumbite structure had an average particle diameter of 0.5 ⁇ m and an average thickness of 0.2 ⁇ m.
  • the ferrite particles with magnetoplumbite structure obtained in Production Example 1 were filled in a graphite mold and pressurized to 40 MPa. While keeping the pressurized condition, an electric current of 800 A (voltage applied: 3 V) was supplied to the particles filled in the mold to generate an electric spark therebetween, thereby heating the particles to 900°C for about 5 minutes. After keeping the temperature of 900°C for 5 minutes, the particles were allowed to stand for natural cooling. The obtained sintered product was held in air at 800°C for 2 hours to remove carbon adhered to the surface thereof.
  • 800 A voltage applied: 3 V
  • the thus obtained sintered magnet composed of ferrite particles with magnetoplumbite structure had a density of 5,050 kg/m 3 , a magnetization value of 61.4 Am 2 /kg, a coercive force of 279 kA/m and a magnetic flux density of 390 mT.
  • Example 2 The same procedure as defined in Example 1 was conducted except that composition of ferrite particles with magnetoplumbite structure, sintering temperature, sintering time and amount of growth inhibitor added were varied, thereby producing a sintered magnet composed of ferrite particles with magnetoplumbite structure.

Landscapes

  • Engineering & Computer Science (AREA)
  • Chemical & Material Sciences (AREA)
  • Manufacturing & Machinery (AREA)
  • Ceramic Engineering (AREA)
  • Materials Engineering (AREA)
  • Structural Engineering (AREA)
  • Organic Chemistry (AREA)
  • Power Engineering (AREA)
  • Inorganic Chemistry (AREA)
  • Hard Magnetic Materials (AREA)
  • Manufacturing Cores, Coils, And Magnets (AREA)

Abstract

A process for producing a sintered magnet composed of ferrite particles with magnetoplumbite structure exhibiting a large magnetic flux density and a high coercive force, at a relatively low temperature for a short period of time by filling ferrite particles with magnetoplumbite structure produced by a wet-method, in a mold; and supplying an electric current to the ferrite particles with magnetoplumbite structure filled in the mold under a pressure.

Description

  • The present invention relates to a process for producing a magnetoplumbite-type ferrite sintered magnet, and more particularly, to a process for producing a magnetoplumbite-type ferrite sintered magnet (sintered magnet composed of ferrite particles with magnetoplumbite structure) having a large density and a small crystallite size, at a low temperature for a short period of time.
  • The sintered magnet composed of ferrite particles with magnetoplumbite structures have advantages such as good chemical stability and low production costs and, therefore, have been widely used in various applications such as motors, electronic devices and the like.
  • With recent tendency toward miniaturization and light weight of these devices, it has been required to reduce the size of the magnetoplumbite-type ferrite sintered magnet used therein. For this reason, it has been demanded to provide such a magnetoplumbite-type ferrite sintered magnet exhibiting higher magnetic properties, especially a larger magnetic flux density Bs and a higher coercive force Hc. To meet the demand, it is necessary to sinter magnetoplumbite-type ferrite particles into a high-density body since the magnetic flux density Bs of the magnetoplumbite-type ferrite sintered magnet depends on the density thereof.
  • Conventionally, the magnetoplumbite-type ferrite sintered magnet has been produced by the following method. First, raw materials such as oxides and carbonates containing metal elements as constituents of ferrite particles with magnetoplumbite structure, are mixed together. The resultant mixture is calcined in an electric furnace and then pulverized. The obtained particles are wet-molded under a magnetic field. Then, the obtained molded product is sintered in air at a temperature of 1180 to 1,230°C to produce the magnetoplumbite-type ferrite sintered magnet (Japanese Patent Application Laid-Open (KOKAI) No. 10-149910(1998)).
  • However, in the above-described conventional production method, when the particles are sintered at such a high temperature, the particles undergo excessive growth, so that a crystallite size thereof increases beyond the critical single domain particle diameter (about 0.9 µm). As a result, the obtained sintered magnet is deteriorated in coercive force. In order to prevent the excessive growth of the particles, it has been attempted to conduct a method of adding SiO2 or CaCO3 as a growth inhibitor to the particles, pulverizing the particles and then sintering the pulverized particles to form a sintered magnet. The addition of the growth inhibitor is effective to prevent the growth of particles and improve the coercive force of the obtained sintered magnet. However, since SiO2 or CaCO3 added as the growth inhibitor is a non-magnetic substance, the obtained sintered magnet tends to be deteriorated in magnetic flux density Bs.
  • Specifically, in the production of the magnetoplumbite-type ferrite sintered magnet, it is difficult to enhance both the magnetic flux density and coercive force thereof, because the improvement of one property inevitably causes deterioration of the other property. Such a contradictory relation between these properties is one reason for hindering the reduction in size of the magnetoplumbite-type ferrite sintered magnet.
  • As a result of the present inventors' earnest studies to solve the above problem, it has been found that by sintering ferrite particles with magnetoplumbite structure under pressure while applying an electric current thereto, the obtained sintered magnet composed of ferrite particles with magnetoplumbite structure can exhibit a large magnetic flux density and a high coercive force. The present invention has been attained based on the above finding.
  • An object of the present invention is to provide a process for producing a sintered magnet composed of ferrite particles with magnetoplumbite structure exhibiting a larger magnetic flux density and a high coercive force, at a relatively low temperature for a short period of time.
  • To accomplish the aim, in a first aspect of the present invention, there is provided a process for producing a sintered magnet composed of ferrite particles with magnetoplumbite structure, comprising:
  • filling ferrite particles with magnetoplumbite structure produced by a wet-method, in a mold; and
  • supplying an electric current through the ferrite particles with magnetoplumbite structure filled in mold under a pressure to sinter the ferrite particles with magnetoplumbite structure.
  • In a second aspect of the present invention, there is provided a process for producing a sintered magnet composed of ferrite particles with magnetoplumbite structure, comprising:
  • filling ferrite particles with magnetoplumbite structure produced by a wet-method, in a mold; and
  • supplying an electric current of 100 to 2,000 A at a voltage of 1 to 10 V to the ferrite particles with magnetoplumbite structure filled in the mold under a pressure of 5 to 500 MPa when measured at the surface of a sample compact in the mold, to sinter the ferrite particles with magnetoplumbite structure.
  • In a third aspect of the present invention, there is provided a process for producing a sintered magnet composed of ferrite particles with magnetoplumbite structure, comprising:
  • filling in a mold, ferrite particles with magnetoplumbite structure produced by a wet-method, which have an average particle diameter of 0.1 to 0.9 µm, and a composition represented by the formula: SrO•nFe2O3 wherein a part of Sr may be substituted with Ba, Pb, La, Nd or Pr; a part of Fe may be substituted with Ni, Mn, Ti, Co, Zn, Al or Sn; and n is 5.5 to 6.2; and
  • supplying an electric current of 500 to 1,500 A at a voltage of 1 to 5 V to the ferrite particles with magnetoplumbite structure while applying thereto a pressure of 10 to 200 MPa when measured at the surface of a sample compact in the mold, to sinter the ferrite particles with magnetoplumbite structure.
  • The present invention will now be described in detail below. The ferrite particles with magnetoplumbite structure used in the present invention have a composition represented by the formula: SrO•nFe2O3 wherein a part of Sr may be substituted with Ba, Pb, La, Nd or Pr; a part of Fe may be substituted with Ni, Mn, Ti, Co, Zn, Al or Sn; and n is 5.5 to 6.2.
  • The upper limit of Sr amount substituted with Ba, Pb, La, Nd or Pr is preferably 70 mol%, more preferably 50 mol %, and the upper limit of Fe amount substituted with Ni, Mn, Ti, Co, Zn, Al or Sn is preferably 40 mol%, more preferably 30 mol%. In the consideration of the improvement of the magnetization value, it is preferred to substitute more than 0 and not more than 40 mol% of Sr with La and to substitute more than 0 and not more than 3.3 mol% of Fe with Zn.
  • When the composition of the ferrite particles with magnetoplumbite structure does not satisfy the above-specified formula, it is difficult to obtain the aimed sintered magnet composed of ferrite particles with magnetoplumbite structure having a large magnetic flux density and a high coercive force.
  • The ferrite particles with magnetoplumbite structure may be produced by a known wet-method, more specifically, by mixing a strontium compound and an iron compound together in a solution so as to constitute the above-specified composition; adding sodium hydroxide, potassium hydroxide, etc. to the mixture, thereby causing Sr2+ ions and Fe3+ ions to be precipitated; and then heating the resultant precipitates in an autoclave at about 200°C for subjecting the particles to hydrothermal treatment. Alternatively, there may also be used particles obtained by calcining the precipitates of Sr2+ ions and Fe3+ ions. For example, there may be used fine ferrite particles with magnetoplumbite structure obtained by mixing a strontium compound and an iron compound together in a solution so as to constitute the above-specified composition; adding sodium carbonate, potassium carbonate, etc. to the mixture, thereby causing Sr2+ ions and Fe3+ ions to be precipitated; and then calcining the resultant precipitates at a temperature of about 700 to 1,000°C.
  • The ferrite particles with magnetoplumbite structure produced by the wet-method according to the present invention have an average particle diameter of usually not more than 0.9 µm, preferably 0.1 to 0.9 µm. When the average particle diameter is more than 0.9 µm, the obtained sintered magnet has a crystallite size larger than its critical single domain particle diameter, so that the coercive force thereof tends to be deteriorated. The average thickness of the ferrite particles with magnetoplumbite structure produced by the wet-method according to the present invention is preferably 0.005 to 0.6 µm, more preferably 0.01 to 0.45 µm.
  • In order to prevent the obtained sintered magnet composed of ferrite particles with magnetoplumbite structure using the particles produced by the wet-method from being deteriorated in coercive force or the like, a growth inhibitor such as SiO2 and/or CaCO3 may be mixed with the ferrite particles with magnetoplumbite structure using a ball mill, etc. before sintering. The amount of SiO2 added is preferably not more than 2 % by weight, more preferably not more than 1 % by weight based on the weight of the ferrite particles with magnetoplumbite structure. The amount of CaCO3 added is preferably not more than 2.5 % by weight, more preferably not more than 1.5 % by weight based on the weight of the ferrite particles with magnetoplumbite structure. The amount of mixture of SiO2 and CaCO3 added is preferably not more than 4.5 % by weight, more preferably not more than 2.5 % by weight based on the weight of the ferrite particles with magnetoplumbite structure. The preferable weight ratio of CaCO3 to SiO2 in the mixture thereof 1:1 to 4:1, more preferably 1:1 to 3:1.
  • The ferrite particles with magnetoplumbite structure produced by the wet-method are then filled in a mold, and supplied with an electric current under pressure, thereby sintering the ferrite particles with magnetoplumbite structure. In general, this method is called "spark plasma sintering method". As materials of the mold used in the above sintering method, graphite or the like may be used because of a high electrical conductivity, a low chemical reactivity with ferrite and inexpensiveness thereof.
  • The pressure applied to the ferrite particles with magnetoplumbite structure filled in the mold is usually 5 to 500 MPa, preferably 10 to 200 MPa when measured at the surface of a sample compact in the mold. When the applied pressure is less than 5 MPa, it is difficult to sinter the ferrite particles with magnetoplumbite structure. As a result, the obtained sintered magnet has a density of less than 5,000 kg/m3, resulting in insufficient strength thereof. In addition, the sintered magnet composed of ferrite particles with magnetoplumbite structure having such a low density fails to show a large magnetic flux density. The pressure of 500 MPa is sufficient to sinter the ferrite particles with magnetoplumbite structure. Therefore, in the consideration of economy, it is unnecessary to use such a large pressure exceeding 500 MPa.
  • The electric current applied to the ferrite particles with magnetoplumbite structure is usually 100 to 2,000 A, preferably 500 to 1,500 A. When the electric current applied is less than 100 A, it is difficult to sinter the ferrite particles with magnetoplumbite structure. As a result, the obtained sintered magnet has a density of less than 5,000 kg/m3, resulting in insufficient strength thereof. In addition, the sintered magnet composed of ferrite particles with magnetoplumbite structure having such a low density fails to show a large magnetic flux density. The sintering of the ferrite particles with magnetoplumbite structure can sufficiently proceed by applying the electric current of 2,000 A thereto. Therefore, in the consideration of economy, it is unnecessary to apply such a large electric current exceeding 2,000 A.
  • The voltage applied to the ferrite particles with magnetoplumbite structure is usually 1 to 10 V, preferably 1 to 5 V. When the voltage applied is less than 1 V, it is difficult to sinter the ferrite particles with magnetoplumbite structure. As a result, the obtained sintered magnet has a density of less than 5,000 kg/m3, resulting in insufficient strength thereof. In addition, the sintered magnet composed of ferrite particles with magnetoplumbite structure having such a low density fails to show a large magnetic flux density. The sintering of the ferrite particles with magnetoplumbite structure can sufficiently proceed by applying the voltage of 10 V thereto. Therefore, in the consideration of economy, it is unnecessary to apply such a large voltage exceeding 10 V.
  • The sintering temperature is usually 850 to 1,050°C, preferably 875 to 1,025°C. When the sintering temperature is less than 850°C, it is difficult to sinter the ferrite particles with magnetoplumbite structure. As a result, the obtained sintered magnet has a density of less than 5,000 kg/m3, resulting in insufficient strength thereof. In addition, the sintered magnet composed of ferrite particles with magnetoplumbite structure having such a low density fails to show a large magnetic flux density. When the sintering temperature is more than 1,050°C, the growth of the ferrite particles with magnetoplumbite structure proceeds excessively, so that the crystallite size thereof exceeds the critical single domain particle diameter (about 0.9 µm), resulting in deteriorated coercive force of the obtained sintered magnet.
  • The sintering time is usually 1 to 15 minutes, preferably 1 to 10 minutes. When the sintering time is less than one minute, it is difficult to sinter the ferrite particles with magnetoplumbite structure. As a result, the obtained sintered magnet has a density of less than 5,000 kg/m3, resulting in insufficient strength thereof. In addition, the sintered magnet composed of ferrite particles with magnetoplumbite structure having such a low density fails to show a large magnetic flux density. The sintering time of 15 minutes is sufficient to sinter the ferrite particles with magnetoplumbite structure. Therefore, in the consideration of economy, it is unnecessary to use such a long sintering time beyond 15 minutes.
  • The sintering treatment may be usually conducted in a non-reducing atmosphere, preferably in an oxidative atmosphere. The pressure of the specific atmosphere during the sintering treatment is not particularly restricted, and it is preferred that the sintering treatment be conducted under atmospheric pressure.
  • When the ferrite particles with magnetoplumbite structure are sintered by the above spark plasma sintering method, it is possible to obtain the aimed sintered magnet composed of ferrite particles with magnetoplumbite structure capable of exhibiting a large density and a small crystallite size as well as a large magnetic flux density and a high coercive force. More specifically, in the case of the above spark plasma sintering method used in the present invention, it is suggested that when applying the above-specified amount of electric current to the ferrite particles with magnetoplumbite structure filled in the mold under pressure, the spark plasma is generated within the mold and directly acts between the particles, unlike the conventional method in which a molded product composed of the ferrite particles with magnetoplumbite structure is sintered in an electric furnace such as Fisher furnace at a temperature of more than 1,080°C for not less than 30 minutes. Thus, in the present invention, since the ferrite particles with magnetoplumbite structure are sintered at a relatively low temperature for a short period of time, the ferrite particles with magnetoplumbite structure can be prevented from suffering from excessive growth. As a result, it becomes possible to obtain a sintered magnet composed of ferrite particles with magnetoplumbite structure having a crystallite size not more than the critical single domain particle diameter (0.9 µm), a density of not less than 5,000 kg/m3, preferably 5,000 to 5,150 kg/m3, a magnetization value of 60 to 70 Am2/kg, a coercive force of 100 to 400 kA/m and a magnetic flux density of 350 to 450 mT.
  • In the present invention, since the ferrite particles with magnetoplumbite structure are sintered together at a relatively low temperature for a short period of time by the spark plasma sintering method, the growth of the ferrite particles with magnetoplumbite structure can be effectively inhibited. As a result, it is possible to obtain the aimed sintered magnet composed of ferrite particles with magnetoplumbite structure having a small crystallite size and a high density as well as a large magnetic flux density and a high coercive force.
  • EXAMPLES
  • The present invention will be described in more detail by reference to the following examples. However, these examples are only illustrative and not intended to limit the present invention thereto.
  • (1) The shape of the ferrite particles with magnetoplumbite structure was observed by a field emission-type scanning electron microscope "S-800" manufactured by Hitachi Limited.
  • (2) The magnetization value σs and coercive force Hc of the ferrite particles with magnetoplumbite structure were measured by a vibratiin sample megnetometer "BHV-35" manufactured by Riken Denshi Co., Ltd. by applying a magnetic field of 1,193 kA/m (15 kOe) thereto. The sample measured each had a disk-like shape having a diameter of 7 mm and a thickness of 3 mm. The magnetic field was applied in the direction parallel to the disk flat surface.
  • (3) The density 'd' of the sintered magnet composed of ferrite particles with magnetoplumbite structure was measured by Archimedes method.
  • (4) The magnetic flux density Bs of the sintered magnet composed of ferrite particles with magnetoplumbite structure was calculated from the above-measured magnetization value σs and density d according to the following formula: Bs = 4π × σs × d
  • Production Example 1:
  • An aqueous mixed solution containing SrCl2•6H2O and Fe(NO3)3•9H2O was prepared such that the molar ratio of Fe3+ to Sr2+ was 11.4:1. An aqueous NaOH solution was then added to the aqueous mixed solution in an amount not less than that required for neutralizing the Sr and Fe compounds so as to allow Sr2+ ions and Fe3+ ions to be precipitated. The obtained precipitates were treated in an autoclave at 200°C under 20 atm for 5 hours. The resultant reaction product was washed with water, filtered out and then dried, thereby obtaining ferrite particles with magnetoplumbite structure. It was confirmed that the thus obtained ferrite particles with magnetoplumbite structure had an average particle diameter of 0.25 µm and an average thickness of 0.08 µm.
  • Production Example 2:
  • An aqueous mixed solution containing SrCl2•6H2O and Fe(NO3)3•9H2O was prepared such that the molar ratio of Fe3+ to Sr2+ was 11.4:1. Na2CO3 was added to the aqueous mixed solution in an amount not less than that required for neutralizing the Sr and Fe compounds so as to allow Sr2+ ions and Fe3+ ions to be precipitated. The obtained precipitates were calcined in air at 1,000°C for 3 hours, thereby obtaining ferrite particles with magnetoplumbite structure. It was confirmed that the thus obtained ferrite particles with magnetoplumbite structure had an average particle diameter of 0.5 µm and an average thickness of 0.2 µm.
  • Example 1:
  • The ferrite particles with magnetoplumbite structure obtained in Production Example 1 were filled in a graphite mold and pressurized to 40 MPa. While keeping the pressurized condition, an electric current of 800 A (voltage applied: 3 V) was supplied to the particles filled in the mold to generate an electric spark therebetween, thereby heating the particles to 900°C for about 5 minutes. After keeping the temperature of 900°C for 5 minutes, the particles were allowed to stand for natural cooling. The obtained sintered product was held in air at 800°C for 2 hours to remove carbon adhered to the surface thereof.
  • It was confirmed that the thus obtained sintered magnet composed of ferrite particles with magnetoplumbite structure had a density of 5,050 kg/m3, a magnetization value of 61.4 Am2/kg, a coercive force of 279 kA/m and a magnetic flux density of 390 mT.
  • Examples 2 to 6 and Comparative Examples 1 to 4:
  • The same procedure as defined in Example 1 was conducted except that composition of ferrite particles with magnetoplumbite structure, sintering temperature, sintering time and amount of growth inhibitor added were varied, thereby producing a sintered magnet composed of ferrite particles with magnetoplumbite structure.
  • Production conditions are shown in Tables 1 and 3, and various properties of the obtained sintered magnets are shown in Tables 2 and 4.
    Figure 00160001
    Figure 00160002
    Figure 00170001
    Figure 00170002
    Figure 00180001
    Figure 00180002
    Figure 00190001
    Figure 00190002
    Figure 00200001
    Figure 00200002

Claims (5)

  1. A process for producing a sintered magnet comprising ferrite particles with magnetoplumbite structure, comprising:
    placing said ferrite particles in a mold; and then
    supplying an electric current of 100 to 2,000 A at a voltage of 1 to 10 V to said ferrite particles under a pressure of 5 to 500 MPa at the surface of a sample compact in the mold, to sinter said ferrite particles.
  2. A process according to claim 1, wherein sintering is conducted at a temperature of 850 to 1,050°C for 1 to 15 minutes..
  3. A process according to claim 1 or 2, wherein said pressure is 10 to 200 MPa, said electric current is 500 to 1,500 A, and said voltage is 1 to 5 V.
  4. A process according to claim 1, 2 or 3, wherein said ferrite particles have an average particle diameter of 0.1 to 0.9 µm, and a composition represented by the formula: SrO•nFe2O3 wherein a part of Sr may be substituted with Ba, Pb, La, Nd or Pr; a part of Fe may be substituted with Ni, Mn, Ti, Co, Zn, Al or Sn; and n is 5.5 to 6.2.
  5. A process according to any preceding claim, wherein sintering is conducted at a temperature of 875 to 1,025 °C for 1 to 10 minutes.
EP01304165A 2000-05-11 2001-05-09 Process for producing magnetoplumbite-type ferrite sintered magnet Withdrawn EP1153900A3 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2000138325 2000-05-11
JP2000138325 2000-05-11

Publications (2)

Publication Number Publication Date
EP1153900A2 true EP1153900A2 (en) 2001-11-14
EP1153900A3 EP1153900A3 (en) 2003-08-06

Family

ID=18645955

Family Applications (1)

Application Number Title Priority Date Filing Date
EP01304165A Withdrawn EP1153900A3 (en) 2000-05-11 2001-05-09 Process for producing magnetoplumbite-type ferrite sintered magnet

Country Status (2)

Country Link
US (1) US20020005603A1 (en)
EP (1) EP1153900A3 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN105122389A (en) * 2013-04-03 2015-12-02 户田工业株式会社 Ferrite particle powder for bonded magnet, resin composition for bonded magnet, and molded body using same

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2015050119A1 (en) 2013-10-02 2015-04-09 戸田工業株式会社 Ferrite particle powder for bonded magnet, resin composition for bonded magnet, and molded article using ferrite particle powder and resin composition
CN109574083B (en) * 2018-12-04 2021-06-25 浙江安特磁材股份有限公司 Rubber-plastic ferrite magnetic powder and preparation method thereof, magnetic product and application

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB825251A (en) * 1956-11-16 1959-12-09 Badische Anilin & Soda Fabric Improvements in the production of ferrites
EP0503639A1 (en) * 1991-03-15 1992-09-16 Sony Corporation Polycristalline ferrite materials
JPH0722229A (en) * 1993-06-16 1995-01-24 Idemitsu Material Kk Production of oxide magnetic material
JPH11121218A (en) * 1997-10-15 1999-04-30 Tokin Corp Ferrite permanent magnet and manufacture thereof

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP3256377B2 (en) * 1993-08-12 2002-02-12 日立金属株式会社 Manufacturing method of ferrite magnet

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB825251A (en) * 1956-11-16 1959-12-09 Badische Anilin & Soda Fabric Improvements in the production of ferrites
EP0503639A1 (en) * 1991-03-15 1992-09-16 Sony Corporation Polycristalline ferrite materials
JPH0722229A (en) * 1993-06-16 1995-01-24 Idemitsu Material Kk Production of oxide magnetic material
JPH11121218A (en) * 1997-10-15 1999-04-30 Tokin Corp Ferrite permanent magnet and manufacture thereof

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
RYU J R ET AL: "Microstructure and mechanical properties of nanocrystalline Al-Ti alloys consolidated by plasma activated sintering" JOURNAL OF ALLOYS AND COMPOUNDS, ELSEVIER SEQUOIA, LAUSANNE, CH, vol. 296, no. 1-2, 10 January 2000 (2000-01-10), pages 157-165, XP004253806 ISSN: 0925-8388 *

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN105122389A (en) * 2013-04-03 2015-12-02 户田工业株式会社 Ferrite particle powder for bonded magnet, resin composition for bonded magnet, and molded body using same

Also Published As

Publication number Publication date
EP1153900A3 (en) 2003-08-06
US20020005603A1 (en) 2002-01-17

Similar Documents

Publication Publication Date Title
EP1798211B1 (en) Ferrite magnetic material
EP2043112B1 (en) Ferrite sintered magnet
JP4919636B2 (en) Oxide magnetic material and sintered magnet
EP1808422B1 (en) Oxide magnetic material and sintered magnet
WO2011001831A1 (en) Ferrite sintered magnet producing method and ferrite sintered magnet
EP1684315A2 (en) Ferrite magnet and method for producing same
EP2892058B1 (en) Ferrite calcined body, method for producing ferrite sintered magnet, and ferrite sintered magnet
BRPI0620713A2 (en) magnetic oxide material
CN111755193B (en) Ferrite sintered magnet and rotating electrical machine provided with same
JP2009120442A (en) Oxide magnetic material, its producing method and sintered magnet
JPH10149910A (en) Ferrite magnet and its manufacturing method
JP4194013B2 (en) Ferrite magnet manufacturing method
WO2001035424A1 (en) Ferrite magnet powder and magnet using the magnet powder, and method for preparing them
CN111747737B (en) Ferrite sintered magnet and rotary electric device provided with same
US20020005603A1 (en) Process for producing magnetoplumbite-type ferrite sintered magnet
JP3835729B2 (en) Ferrite sintered magnet and manufacturing method thereof
JP3506174B2 (en) Method for producing ferrite magnet and powder thereof
JP2008187184A (en) Production process of ferrite magnet
JP2002141212A (en) Rotating machine
JP2006203260A (en) Ferrite magnet
JP2002029829A (en) Method for manufacturing sintered magnetoplumbite type ferrite magnet
JPH11307331A (en) Ferrite magnet
WO2003056578A1 (en) Magnetoplumbite-type ferrite magnet having improved properties and preparation thereof
JP3944860B2 (en) Ferrite magnet powder
JP2006002187A (en) Sm-Fe-N-BASED MAGNETIC PARTICLE POWDER, AND BOND MAGNET CONTAINING THE Sm-Fe-N-BASED MAGNETIC PARTICLE POWDER

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

AK Designated contracting states

Kind code of ref document: A2

Designated state(s): AT BE CH CY DE DK ES FI FR GB GR IE IT LI LU MC NL PT SE TR

AX Request for extension of the european patent

Free format text: AL;LT;LV;MK;RO;SI

PUAL Search report despatched

Free format text: ORIGINAL CODE: 0009013

AK Designated contracting states

Designated state(s): AT BE CH CY DE DK ES FI FR GB GR IE IT LI LU MC NL PT SE TR

AX Request for extension of the european patent

Extension state: AL LT LV MK RO SI

AKX Designation fees paid
STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: THE APPLICATION IS DEEMED TO BE WITHDRAWN

REG Reference to a national code

Ref country code: DE

Ref legal event code: 8566

18D Application deemed to be withdrawn

Effective date: 20031202